Study of Atorvastatin/Fenofibrate (LCP-AtorFen) Combination Therapy in Dyslipidemia

NCT00504829 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 220

Last updated 2020-02-17

Study results available
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Summary

The current study is designed to test the efficacy, safety and tolerability of LCP-AtorFen, a combination of atorvastatin and fenofibrate.

Conditions

Interventions

DRUG

LCP-AtorFen

40mg atorvastatin combined with 100mg fenofibrate in a tablet for once daily treatment of dyslipidemia and mixed dyslipidemia

DRUG

atorvastatin

dyslipidemia and mixed dyslipidemia

DRUG

fenofibrate

dyslipidemia and mixed dyslipidemia

Sponsors & Collaborators

  • Veloxis Pharmaceuticals

    lead INDUSTRY

Principal Investigators

  • Jeff Geohas, MD · Radiant Research

  • Dennis McCluskey, MD · Radiant Research

  • Harry Geisberg, MD · Radiant Research

  • Chivers Woodruff, Jr, MD · Radiant Research

  • Michael Noss, MD · Radiant Research

  • Michele Reynolds, MD · Radiant Research

  • James Zavoral, MD · Radiant Research

  • Randall Severance, MD · Radiant Research

  • Stephen Halpern, MD · Radiant Research

  • Linda Murray, MD · Radiant Research

  • Wayne Larson, MD · Radiant Research

  • Timothy Howards, MD · Medical Affiliated Research Center, Inc.

  • Cynthia Strout, MD · Coastal Carolina Research Center

  • Mark Kipnes, MD · Diabetes and Glandular Research Center, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-07-31
Primary Completion
2008-02-29
Completion
2008-07-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00504829 on ClinicalTrials.gov